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Effect of tDCS on the improvement of motor and cognitive function in patients with stroke and its brain network mechanism

Research and application of active rehabilitation technology for cerebrovascular disease based on BCI

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031314
Enrollment
Unknown
Registered
2020-03-27
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

Control group:Routine rehabilitation therapy and routine physical factor therapy
Single channel tDCS group:Single channel tDCS therapy on the basis of routine comprehensive rehabilitation therapy
Multi-channel tDCS group:Multi-channel tDCS therapy on the basis of routine comprehensive rehabilitation therapy

Sponsors

The First Hospital Affiliated to AMU
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with cerebral hemorrhage and cerebral infarction for the first time confirmed by CT or MRI or with previous lacunar cerebral infarction but without sequelae; 2. 18 to 70 years of age; 3. course of disease: 2 weeks to 3 months; 4. Patients with hemiplegia of one limb, and the muscle tension on the affected side is graded = II; 6. Patients who agree and sign informed consent for treatment.

Exclusion criteria

Exclusion criteria: 1. The vital signs are still unstable; 2. Those who use implantable electronic devices (such as pacemakers); 3. Those who have metal implants such as stents; 4. Patients who are critically ill or have important organ failure; 5. Pregnant women; 6. Patients with severe allergy to electrode patch, local skin injury or inflammation, and those with hyperalgesia in the stimulating area; 7. Epilepsy or patients with diagnosed secondary epilepsy; 8. Tumor patients; 9. Patients with severe cognitive impairment (MMSE score < 24 points); 10. With previous medical history of mental disorders and medication history that caused symptoms of mental disorders.

Design outcomes

Primary

MeasureTime frame
MoCA;HAMD;ARAT;EEG;MRI;Basic function evaluation;

Countries

China

Contacts

Public ContactJingming Hou

The First Hospital Affiliated to AMU

hjmkfk@163.com+86 17723562203

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026